Mcgaw, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Mcgaw, Inc. - FDA 510(k) Cleared Devices
13
Total
13
Cleared
0
Denied
Mcgaw, Inc. has 13 FDA 510(k) cleared general hospital devices. Based in Irvine, US.
Historical record: 13 cleared submissions from 1991 to 1997.
Browse the complete list of FDA 510(k) cleared general hospital devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Mcgaw, Inc.
13 devices
Cleared
Oct 07, 1997
MILLENNIUM CRT INFUSION PUMP AND MILLENNIUM CRT INFUSION PUMP ADMINISTRATION...
General Hospital
83d
Cleared
Mar 06, 1996
SAFELINE I.V. BAG ACCESS DEVICE
General Hospital
89d
Cleared
Mar 06, 1996
SAFELINE MULTIDOSE VIAL ADAPTER
General Hospital
89d
Cleared
Nov 29, 1994
SAFELINE SYSTEM TURN LOCK CANNULA
General Hospital
259d
Cleared
Apr 13, 1994
INTRAVASCULAR ADMINISTRATION SET
General Hospital
344d
Cleared
Mar 07, 1994
SAFELINE SYSTEM IV ADMINISTRATION SETS & COMPONENT
General Hospital
354d
Cleared
Jan 26, 1994
IRRIGATION ACCESS CAP
General Hospital
230d
Cleared
Jun 04, 1993
HORIZON PUMP Y-TYPE BLOOD SET
General Hospital
365d
Cleared
Jul 30, 1992
MODIFICATION TO IV SPIKE
General Hospital
141d
Cleared
Dec 18, 1991
MODIFIED VOLUMETRIC INFUSION PUMP
General Hospital
138d
Cleared
Sep 06, 1991
VOLUMETRIC INFUSION PUMP, MODIFICATION
General Hospital
66d
Cleared
Jun 24, 1991
INTERVASCULAR ADMINSTRATION SET
General Hospital
67d